Atelocollagen Enhanced Osteogenesis in a Geometric Structured Beta-TCP Scaffold by VEGF Induction

K. Yagami, Sunao Sadaoka, Hiroshi Nakamura, S. Komatsu, J. Onodera, Masahiko Suzuki, Y. Kuboki
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引用次数: 1

Abstract

Abstract In order to establish the convertibility of a host for bone augmentation, we herein developed a new honeycombshaped β-tricalcium phosphate (37H) using atelocollagen as a scaffold, which exhibited unique geometric properties for in vitro and in vivo studies. Human mesenchymal stem cells (MSC) were cultured with 37H or atelocollagen-coated honeycomb-shaped β-tricalcium phosphate (Col37H), and their osteoblastic differentiation was then analyzed. Atelocollagen promoted cell adhesion and formation of vessel-like structures in the tunnels of scaffolds of cultured MSC. The mRNA expression levels of type I collagen, osteocalcin, and VEGF were greater in MSC cultured with Col37H than with 37H. Bone generation with Col37H in the rat calvaria was greater than with 37H, and this was attributed to early vessel construction. A large number of blood vessels invaded tunnels from the periosteum and existing bone surface. A strong VEGF signal was detected immediately before the new bone surface in the tunnels of Col37H. These results indicate that the addition of atelocollagen to Col37H has potential in the construction of functional artificial bone.
血管内皮生长因子诱导胶原蛋白促进几何结构β - tcp支架成骨
为了建立骨增强宿主的可转换性,我们在此开发了一种新型蜂窝状的β-磷酸三钙(37H),该支架以胶原为支架,在体外和体内研究中均表现出独特的几何特性。用37H或胶原包被蜂窝状β-磷酸三钙(Col37H)培养人间充质干细胞(MSC),观察其成骨分化情况。胶原蛋白促进细胞黏附和血管样结构的形成。Col37H培养的MSC中I型胶原、骨钙素和VEGF mRNA表达水平高于37H培养的MSC。大鼠颅骨中Col37H的骨生成大于37H,这归因于早期血管构建。大量血管从骨膜和现有骨表面侵入隧道。在Col37H的隧道中,在新骨表面形成之前检测到强烈的VEGF信号。这些结果表明,在Col37H中添加间胶原具有构建功能性人工骨的潜力。
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